Evidence map›Paper›PMID 37298266›Full record

ArticleInternational journal of molecular sciences2023

Molecular Signatures in Swine Innate and Adaptive Immune Responses to African Swine Fever Virus Antigens p30/p54/CD2v Expressed Using a Highly Efficient Semliki Forest Virus Replicon System.

Mei Huang, Hanghui Zheng, Weixiong Tan, Chengwei Xiang, Niran Fang, Wenting Xie, Lianghai Wen, Dingxiang Liu, Ruiai Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Mei HuangZhaoqing Institute of Biotechnology Co., Ltd., Zhaoqing 526238, China.
Hanghui ZhengZhaoqing Institute of Biotechnology Co., Ltd., Zhaoqing 526238, China.
Weixiong TanZhaoqing Institute of Biotechnology Co., Ltd., Zhaoqing 526238, China.
Chengwei XiangZhaoqing Branch Center of Guangdong Laboratory for Lingnan Modern Agricultural Science and Technology, Zhaoqing 526000, China.
Niran FangZhaoqing Institute of Biotechnology Co., Ltd., Zhaoqing 526238, China.
Wenting XieCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, China.
Lianghai WenZhaoqing Institute of Biotechnology Co., Ltd., Zhaoqing 526238, China.
Dingxiang LiuZhaoqing Branch Center of Guangdong Laboratory for Lingnan Modern Agricultural Science and Technology, Zhaoqing 526000, China.ORCID 0000-0001-6039-2948
Ruiai ChenZhaoqing Institute of Biotechnology Co., Ltd., Zhaoqing 526238, China.
Zhaoqing University · CNSouth China Agricultural University · CN

Funding

National Natural Science Foundation of China grants 31972660 and 32170152The Key-Area Research and Development Program of Guangdong Province 2019B020211004The Zhaoqing science and technology sub-center project on the research for African swine fever vaccine and rapid detection technology development P20211154-0101
6 · The paper itself

Abstract

African swine fever virus (ASFV) causes a devastating viral hemorrhagic disease in domestic pigs and Eurasian wild boars, posing a foremost threat to the swine industry and pig farming. The development of an effective vaccine is urgently needed, but has been hampered by the lack of an in-depth, mechanistic understanding of the host immune response to ASFV infection and the induction of protective immunity. In this study, we report that immunization of pigs with Semliki Forest Virus (SFV) replicon-based vaccine candidates expressing ASFV p30, p54, and CD2v, as well as their ubiquitin-fused derivatives, elicits T cell differentiation and expansion, promoting specific T cell and humoral immunity. Due to significant variations in the individual non-inbred pigs in response to the vaccination, a personalized analysis was conducted. Using integrated analysis of differentially expressed genes (DEGs), Venn, KEGG and WGCNA, Toll-like receptor, C-type lectin receptor, IL17 receptor, NOD-like receptor and nucleic acid sensor-mediated signaling pathways were demonstrated to be positively correlated to the antigen-stimulated antibody production and inversely correlated to the IFN-γ secreting cell counts in peripheral blood mononuclear cells (PBMCs). An up-regulation of CIQA, CIQB, CIQC, C4BPA, SOSC3, S100A8 and S100A9, and down-regulation of CTLA4, CXCL2, CXCL8, FOS, RGS1, EGR1 and SNAI1 are general in the innate immune response post-the second boost. This study reveals that pattern recognition receptors TLR4, DHX58/DDX58 and ZBP1, and chemokines CXCL2, CXCL8 and CXCL10 may play important roles in regulating this vaccination-stimulated adaptive immune response.

Indexed as

African Swine Fever VirusAnimalsImmunity, HumoralLeukocytes, MononuclearSemliki forest virusSus scrofaSwineadaptive immune responseAfrican swine fever virus (ASFV)differentially expressed genes (DEGs)innate immunityweighted correlation network analysis (WGCNA)

Identifiers

PMID37298266
PMCPMC10253217
OpenAlexW4378529209

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.